How can you avoid risks and consequences when not following GMP change control and deviation procedures?
Good Manufacturing Practice (GMP) is a set of standards and guidelines that ensure the quality, safety, and consistency of pharmaceutical, biotechnology, and medical device products. One of the key aspects of GMP is change control and deviation management, which are processes that document and control any changes or deviations from the approved procedures, specifications, or methods. By following these processes, you can avoid risks and consequences that may compromise the product quality, regulatory compliance, or patient safety. In this article, we will explain why change control and deviation management are important, what are the common types of changes and deviations, and how to implement best practices to prevent and manage them.